Canonical Allele Identifier: CA497694447

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127981C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224662C>A , CM000679.2:g.7224662C>A	GRCh38
NC_000017.10:g.7127981C>A , CM000679.1:g.7127981C>A	GRCh37
NC_000017.9:g.7068705C>A	NCBI36
NG_007975.1:g.9829C>A
NG_008391.2:g.389G>T
NG_033038.1:g.14883G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1699C>A MANE Select	ENSP00000349297.5:p.Arg567=
ENST00000322910.9:c.*1654C>A	ENSP00000325395.5:n.*1654C>A
ENST00000350303.9:c.1633C>A	ENSP00000344152.5:p.Arg545=
ENST00000356839.9:c.1699C>A	ENSP00000349297.5:p.Arg567=
ENST00000542255.6:c.537-53C>A
ENST00000543245.6:c.1768C>A	ENSP00000438689.2:p.Arg590=
ENST00000578033.1:n.30C>A
ENST00000578319.5:n.280C>A
ENST00000578711.1:n.1158C>A
ENST00000578809.5:n.271C>A
ENST00000579425.5:n.815C>A
ENST00000579546.1:c.434C>A
ENST00000583074.5:n.300-53C>A
ENST00000583848.5:c.65C>A	ENSP00000466487.1:p.Thr22Lys
ENST00000583850.5:n.470C>A
ENST00000583858.5:c.630C>A
ENST00000585203.6:n.890C>A
NM_000018.3:c.1699C>A	NP_000009.1:p.Arg567=
NM_001033859.2:c.1633C>A	NP_001029031.1:p.Arg545=
NM_001270447.1:c.1768C>A	NP_001257376.1:p.Arg590=
NM_001270448.1:c.1471C>A	NP_001257377.1:p.Arg491=
XM_006721516.2:c.1679-53C>A	XP_006721579.2:n.1679-53C>A
XM_011523829.1:c.1577-53C>A	XP_011522131.1:n.1577-53C>A
XM_011523830.1:c.1597C>A	XP_011522132.1:p.Arg533=
XR_934021.1:n.1802C>A
XR_934022.1:n.1708C>A
XR_934023.1:n.1688-53C>A
XM_006721516.3:c.1679-53C>A	XP_006721579.2:n.1679-53C>A
XM_011523829.2:c.1577-53C>A	XP_011522131.1:n.1577-53C>A
XM_011523830.2:c.1597C>A	XP_011522132.1:p.Arg533=
XM_024450741.1:c.1687C>A	XP_024306509.1:p.Arg563=
XR_934021.2:n.1754C>A
XR_934022.2:n.1660C>A
XR_934023.2:n.1640-53C>A
NM_000018.4:c.1699C>A MANE Select	NP_000009.1:p.Arg567=
NM_001033859.3:c.1633C>A	NP_001029031.1:p.Arg545=
NM_001270447.2:c.1768C>A	NP_001257376.1:p.Arg590=
NM_001270448.2:c.1471C>A	NP_001257377.1:p.Arg491=